^Grasbon-Frodl EM, Kösel S, Sprinzl M, von Eitzen U, Mehraein P, Graeber MB. Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease. Neurogenetics. April 1999, 2 (2): 121–7. PMID 10369889. doi:10.1007/s100480050063.
^Yoon KL, Aprille JR, Ernst SG. Mitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiency. Biochemical and Biophysical Research Communications. May 1991, 176 (3): 1112–5. PMID 1645537. doi:10.1016/0006-291X(91)90399-R.
^Reference, Genetics Home. MT-TT gene. Genetics Home Reference. [2021-07-25]. (原始内容存档于2020-09-28) (英语).
^Nishino I, Seki A, Maegaki Y, Takeshita K, Horai S, Nonaka I, Goto Y. A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy. Biochemical and Biophysical Research Communications. August 1996, 225 (1): 180–5. PMID 8769114. doi:10.1006/bbrc.1996.1150.